Canonical Allele Identifier: PA2573203333
Gene: CEP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406907
ClinVar RCV Id: RCV001907021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340047.1:p.Ala273Ser
CA354628972
NM_001353118.1:c.817G>T